Variant report

Variant	nsv461169
Chromosome Location	chr4:3429856-3451109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3443453-3443675	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:3445241-3445522	HepG2	liver:	n/a	n/a
3	ATF3	chr4:3445269-3445466	K562	blood:	n/a	n/a
4	BHLHE40	chr4:3445170-3445557	HepG2	liver:	n/a	chr4:3445365-3445381
5	BHLHE40	chr4:3445224-3445543	K562	blood:	n/a	chr4:3445365-3445381
6	BHLHE40	chr4:3434585-3434667	K562	blood:	n/a	n/a
7	BHLHE40	chr4:3445191-3445500	GM12878	blood:	n/a	chr4:3445365-3445381
8	BRCA1	chr4:3445279-3445522	HepG2	liver:	n/a	n/a
9	CCNT2	chr4:3445350-3445426	K562	blood:	n/a	n/a
10	CEBPB	chr4:3438739-3439132	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:3445210-3445549	Hela-S3	cervix:	n/a	n/a
12	CEBPD	chr4:3445106-3445439	HepG2	liver:	n/a	n/a
13	CEBPD	chr4:3443344-3444000	HepG2	liver:	n/a	n/a
14	CHD2	chr4:3443379-3443859	HepG2	liver:	n/a	chr4:3443687-3443697
15	CHD2	chr4:3438705-3439109	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr4:3444625-3444775	HepG2	liver:	n/a	n/a
17	CHD2	chr4:3442759-3442777	HepG2	liver:	n/a	n/a
18	CHD2	chr4:3445341-3445531	HepG2	liver:	n/a	n/a
19	CHD2	chr4:3445219-3445398	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr4:3444229-3444230	HepG2	liver:	n/a	n/a
21	CHD2	chr4:3438403-3438499	Hela-S3	cervix:	n/a	n/a
22	CREB1	chr4:3445232-3445485	A549	lung:	n/a	n/a
23	CTCF	chr4:3445260-3445410	GM12865	blood:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
24	CTCF	chr4:3436600-3436750	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr4:3436820-3436970	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr4:3445206-3445551	LNCaP	prostate:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
27	CTCF	chr4:3447640-3447790	GM12874	blood:	n/a	n/a
28	CTCF	chr4:3445280-3445430	BJ	skin:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
29	CTCF	chr4:3445740-3445890	BJ	skin:	n/a	n/a
30	CTCF	chr4:3445577-3445579	Fibrobl	skin:	n/a	n/a
31	CTCF	chr4:3445300-3445450	AG04449	skin:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
32	CTCF	chr4:3445564-3445565	GM10248	blood:	n/a	n/a
33	CTCF	chr4:3445280-3445430	HEK293	kidney:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
34	CTCF	chr4:3445017-3445550	H1-hESC	embryonic stem cell:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445175-3445188 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
35	CTCF	chr4:3436720-3436870	BJ	skin:	n/a	n/a
36	CTCF	chr4:3445593-3445730	GM19240	blood:	n/a	n/a
37	CTCF	chr4:3445245-3445539	Pancreas_OC	pancreas:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
38	CTCF	chr4:3445300-3445450	HPF	lung:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
39	CTCF	chr4:3444942-3445680	K562	blood:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445175-3445188 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
40	CTCF	chr4:3436655-3436762	GM13977	blood:	n/a	n/a
41	CTCF	chr4:3445280-3445430	HMF	breast:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
42	CTCF	chr4:3445320-3445470	GM12869	blood:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
43	CTCF	chr4:3445078-3445080	HepG2	liver:	n/a	n/a
44	CTCF	chr4:3445260-3445410	GM12866	blood:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
45	CTCF	chr4:3445300-3445450	GM12864	blood:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
46	CTCF	chr4:3445280-3445430	AG09319	gingival:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
47	CTCF	chr4:3436602-3436813	HepG2	liver:	n/a	n/a
48	CTCF	chr4:3445280-3445430	HRPEpiC	eye:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
49	CTCF	chr4:3445069-3445502	A549	lung:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445175-3445188 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
50	CTCF	chr4:3444877-3445778	A549	lung:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445175-3445188 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3450770-3450820	NHBE	bronchial:	n/a
2	chr4:3447935-3447985	A549	lung:	n/a
3	chr4:3449856-3449906	AG04450	lung:	fetal
4	chr4:3450770-3450820	NHBE	bronchial:	n/a
5	chr4:3447935-3447985	A549	lung:	n/a
6	chr4:3449856-3449906	AG04450	lung:	fetal
7	chr4:3449663-3449713	NH-A	brain:	n/a
8	chr4:3447935-3447985	NB4	blood:	n/a
9	chr4:3435449-3435499	BJ	skin:	n/a
10	chr4:3448150-3448200	HCPEpiC	choroid plexus:	n/a
11	chr4:3443608-3443658	HepG2	liver:	n/a
12	chr4:3436404-3436454	SKMC	muscle:	n/a
13	chr4:3436168-3436218	AG09309	skin:	n/a
14	chr4:3433773-3433823	RPTEC	kidney:	n/a
15	chr4:3436404-3436454	ovcar-3	ovarian:	n/a
16	chr4:3443735-3443785	A549	lung:	n/a
17	chr4:3443683-3443733	HCT-116	colon:	n/a
18	chr4:3443694-3443744	U87	brain:	n/a
19	chr4:3442962-3443012	HepG2	liver:	n/a
20	chr4:3447665-3447715	ProgFib	skin:	n/a
21	chr4:3449663-3449713	LNCaP	prostate:	n/a
22	chr4:3450770-3450820	SAEC	small airway:	n/a
23	chr4:3450770-3450820	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:3443656-3443706	LNCaP	prostate:	n/a
25	chr4:3449663-3449713	AG09309	skin:	n/a
26	chr4:3443656-3443706	PFSK-1	brain:	n/a
27	chr4:3435449-3435499	NHBE	bronchial:	n/a
28	chr4:3443683-3443733	AG09319	gingival:	n/a
29	chr4:3450770-3450820	A549	lung:	n/a
30	chr4:3432483-3432533	SKMC	muscle:	n/a
31	chr4:3432546-3432596	AG09319	gingival:	n/a
32	chr4:3436168-3436218	U87	brain:	n/a
33	chr4:3436404-3436454	GM19239	blood:	n/a
34	chr4:3436168-3436218	AG04449	skin:	fetal
35	chr4:3433526-3433576	HNPCEpiC	eye:	n/a
36	chr4:3449300-3449350	SK-N-SH	brain:	n/a
37	chr4:3432483-3432533	HCPEpiC	choroid plexus:	n/a
38	chr4:3449300-3449350	LNCaP	prostate:	n/a
39	chr4:3435498-3435548	NH-A	brain:	n/a
40	chr4:3449856-3449906	Hepatocyte	liver:	n/a
41	chr4:3443625-3443675	GM06990	blood:	n/a
42	chr4:3433773-3433823	SK-N-SH	brain:	n/a
43	chr4:3449663-3449713	SK-N-MC	brain:	n/a
44	chr4:3443683-3443733	NH-A	brain:	n/a
45	chr4:3433526-3433576	PrEC	prostate:	n/a
46	chr4:3446405-3446455	HCF	heart:	n/a
47	chr4:3449663-3449713	AG09319	gingival:	n/a
48	chr4:3443025-3443075	AoSMC	blood vessel:	n/a
49	chr4:3435498-3435548	K562	blood:	n/a
50	chr4:3435525-3435575	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:3432116..3434989-chr4:3463177..3465142,2	MCF-7	breast:
2	chr4:3401369..3402190-chr4:3444884..3445429,2	K562	blood:
3	chr4:3438145..3440558-chr4:3486054..3488354,2	MCF-7	breast:
4	chr4:3417191..3419894-chr4:3434904..3438347,3	MCF-7	breast:
5	chr4:3297878..3299647-chr4:3439847..3442316,2	MCF-7	breast:
6	chr4:3401278..3402259-chr4:3444676..3445847,3	MCF-7	breast:
7	chr4:3439130..3442230-chr4:3483136..3486025,3	MCF-7	breast:
8	chr4:3442877..3445560-chr4:3447912..3450981,3	MCF-7	breast:
9	chr4:3444953..3445626-chr4:3481708..3482572,4	MCF-7	breast:
10	chr4:3347483..3348481-chr4:3444797..3445914,9	MCF-7	breast:
11	chr4:3432863..3436671-chr4:3438111..3441622,5	K562	blood:
12	chr4:3347550..3348452-chr4:3441019..3441869,2	K562	blood:
13	chr4:3428890..3430804-chr4:3441748..3443973,2	MCF-7	breast:
14	chr4:3439707..3441284-chr4:3443467..3445284,2	K562	blood:
15	chr4:3438642..3440686-chr4:3450024..3452220,2	MCF-7	breast:
16	chr4:3438822..3441284-chr4:3443467..3446994,3	K562	blood:
17	chr4:3340754..3343218-chr4:3436055..3438880,2	MCF-7	breast:
18	chr4:3437849..3440325-chr4:3440402..3441941,2	MCF-7	breast:
19	chr12:52607035..52609334-chr4:3440706..3442862,2	MCF-7	breast:
20	chr4:3437849..3440325-chr4:3440402..3441941,2	MCF-7	breast:
21	chr4:3428384..3430154-chr4:3434283..3437033,2	K562	blood:
22	chr4:3432863..3436671-chr4:3438111..3441622,5	K562	blood:
23	chr4:3444972..3445545-chr7:150654913..150655661,2	MCF-7	breast:
24	chr4:3293054..3295146-chr4:3436472..3438232,3	MCF-7	breast:
25	chr4:3387900..3390200-chr4:3439176..3442077,2	MCF-7	breast:
26	chr4:3433662..3435560-chr4:3437260..3439057,2	MCF-7	breast:
27	chr4:3430343..3432771-chr4:3437903..3441095,3	K562	blood:
28	chr4:3438186..3441523-chr4:3461903..3464658,4	MCF-7	breast:
29	chr4:3433662..3435560-chr4:3437260..3439057,2	MCF-7	breast:
30	chr4:3347569..3348482-chr4:3444950..3445609,2	MCF-7	breast:
31	chr4:3355212..3358066-chr4:3437874..3440532,4	MCF-7	breast:
32	chr4:3438758..3441335-chr4:3441966..3444505,4	MCF-7	breast:
33	chr4:3415712..3418675-chr4:3431596..3433223,2	MCF-7	breast:
34	chr4:3416652..3419915-chr4:3441173..3444245,3	MCF-7	breast:
35	chr4:3321370..3323027-chr4:3448401..3450005,2	MCF-7	breast:
36	chr4:3437523..3439091-chr4:3448156..3450987,2	MCF-7	breast:
37	chr4:3428890..3430804-chr4:3441748..3443973,2	MCF-7	breast:
38	chr4:3448773..3453068-chr4:3461459..3466470,7	MCF-7	breast:
39	chr4:3422645..3425998-chr4:3426569..3431321,4	K562	blood:
40	chr4:3437523..3439091-chr4:3448156..3450987,2	MCF-7	breast:
41	chr4:3448881..3451468-chr4:3454721..3457029,2	K562	blood:
42	chr4:3347496..3348411-chr4:3444927..3445862,6	K562	blood:
43	chr4:3401381..3402237-chr4:3444863..3445577,2	MCF-7	breast:
44	chr4:3293753..3295526-chr4:3439987..3441578,2	MCF-7	breast:
45	chr4:3438642..3440686-chr4:3450024..3452220,2	MCF-7	breast:
46	chr4:3351060..3353090-chr4:3436592..3439411,2	MCF-7	breast:
47	chr4:3195267..3196266-chr4:3444903..3445887,5	MCF-7	breast:
48	chr4:3430343..3432771-chr4:3437903..3441095,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS12-1	chr4:3441182-3441640	NONHSAT094871
2	lnc-RGS12-1	chr4:3429816-3429896	NONHSAT094871

Variant related genes	Relation type
HGFAC	TF binding region
HGFAC	CpG island
ENSG00000159788	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000109758	chromatin interactions

Extended variants
information (count: 1293 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2269497	chr4:3429856-3429857	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs138197161	chr4:3429866-3429867	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs373758436	chr4:3429890-3429891	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs376934506	chr4:3429905-3429906	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs371590435	chr4:3429915-3429916	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs553320534	chr4:3429924-3429925	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs374671098	chr4:3429926-3429927	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545024584	chr4:3429927-3429928	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs367595436	chr4:3429930-3429931	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs370177098	chr4:3429932-3429933	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs373892377	chr4:3429938-3429939	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs55827497	chr4:3429942-3429943	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149629037	chr4:3429949-3429950	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs544790631	chr4:3429960-3429961	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs561353666	chr4:3430013-3430014	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530330186	chr4:3430023-3430024	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546947414	chr4:3430026-3430027	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370707564	chr4:3430036-3430037	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs532330002	chr4:3430056-3430057	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs552194032	chr4:3430058-3430059	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs569006629	chr4:3430064-3430065	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374182717	chr4:3430066-3430067	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537981808	chr4:3430082-3430083	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs550735138	chr4:3430099-3430100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs567315423	chr4:3430217-3430218	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs369464208	chr4:3430239-3430240	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373234109	chr4:3430240-3430241	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs528284054	chr4:3430306-3430307	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371903496	chr4:3430360-3430361	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs376574188	chr4:3430371-3430372	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs142314294	chr4:3430406-3430407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs267600139	chr4:3430429-3430430	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs553257302	chr4:3430461-3430462	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs148603274	chr4:3430465-3430466	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569298391	chr4:3430496-3430497	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538632574	chr4:3430541-3430542	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs368898673	chr4:3430576-3430577	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540919261	chr4:3430598-3430599	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs192712259	chr4:3430620-3430621	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544011298	chr4:3430649-3430650	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs1209994	chr4:3430702-3430703	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs561057690	chr4:3430708-3430709	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574886234	chr4:3430766-3430767	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs28484982	chr4:3430770-3430771	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs560400538	chr4:3430779-3430780	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559300976	chr4:3430780-3430781	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs141143466	chr4:3430801-3430802	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs552130787	chr4:3430814-3430815	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1203112	chr4:3430862-3430863	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs182528925	chr4:3430873-3430874	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3399200-3432200	Weak transcription	Right Atrium	heart
2	chr4:3408800-3436600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr4:3411000-3436400	Strong transcription	Fetal Intestine Small	intestine
4	chr4:3411200-3436400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr4:3411200-3436600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr4:3413600-3437000	Strong transcription	Esophagus	oesophagus
7	chr4:3415000-3435600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:3415000-3436400	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr4:3415400-3437000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:3415600-3433600	Weak transcription	Fetal Kidney	kidney
11	chr4:3415800-3436400	Strong transcription	Lung	lung
12	chr4:3416400-3436200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr4:3416400-3436800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:3416600-3435600	Strong transcription	Skeletal Muscle Male	skeletal muscle
15	chr4:3416600-3437800	Weak transcription	Stomach Mucosa	stomach
16	chr4:3416800-3432000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr4:3416800-3436600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr4:3416800-3438400	Weak transcription	NHDF-Ad	bronchial
19	chr4:3417200-3433400	Strong transcription	Stomach Smooth Muscle	stomach
20	chr4:3417200-3435600	Strong transcription	Fetal Intestine Large	intestine
21	chr4:3417200-3444800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr4:3417400-3431000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr4:3417800-3432800	Weak transcription	Small Intestine	intestine
24	chr4:3417800-3435200	Strong transcription	Adipose Nuclei	Adipose
25	chr4:3417800-3435200	Strong transcription	Fetal Brain Female	brain
26	chr4:3418200-3436600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr4:3418200-3438000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:3418200-3438000	Weak transcription	A549	lung
29	chr4:3419000-3434600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr4:3419200-3444600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr4:3419400-3438400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr4:3419600-3435600	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr4:3419600-3438400	Weak transcription	NH-A	brain
34	chr4:3419800-3435200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr4:3419800-3438800	Weak transcription	NHLF	lung
36	chr4:3420000-3437000	Strong transcription	Brain Germinal Matrix	brain
37	chr4:3420200-3438400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:3420400-3435200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:3420400-3436000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:3420400-3436600	Weak transcription	Fetal Brain Male	brain
41	chr4:3420400-3438200	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr4:3420400-3438600	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr4:3420600-3430800	Weak transcription	HSMMtube	muscle
44	chr4:3420600-3435600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:3420600-3436400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr4:3422200-3435200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:3423600-3431400	Weak transcription	Fetal Thymus	thymus
48	chr4:3423600-3437400	Strong transcription	Fetal Stomach	stomach
49	chr4:3424400-3435400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:3425600-3430400	Weak transcription	Placenta Amnion	Placenta Amnion

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